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[ CAS No. 952727-77-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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Chemical Structure| 952727-77-4
Chemical Structure| 952727-77-4
Structure of 952727-77-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 952727-77-4 ]

CAS No. :952727-77-4 MDL No. :MFCD04114807
Formula : C15H11Cl2NO2S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 340.22 Pubchem ID :-
Synonyms :

Safety of [ 952727-77-4 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P310-P330-P332+P313-P337+P313-P361-P403+P233-P405-P501 UN#:2811
Hazard Statements:H301-H311-H315-H319-H331-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 952727-77-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 952727-77-4 ]

[ 952727-77-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 952727-77-4 ]
  • [ 728034-12-6 ]
  • [ 108-91-8 ]
  • 4-(1-cyclohexyl-4-(2,4-dichlorophenyl)-1H-imidazol-5-yl)-1H-pyrrolo[2,3-b]pyridine [ No CAS ]
YieldReaction ConditionsOperation in experiment
2% To a solution of 1 //-pyrrolol 2,3-61 pyridi ne-4-carbaldehyde (42 mg; 0.289 mmol) in tetrahydrofuran (2 mL) was added cyclohexanamine (0.067 mL; 0.600 mmol) and the resulting solution was stirred at 25 Cfor 210 minutes. Then,2,4-dichloro-l-(isocyano(tosyl)methyl)benzene (81 mg; 0.240 mmol), CS2CO3 (117 mg; 0,360 mmol) and boron trifluoride diethyl etherate (0.088 mL; 0.720 mmol) were added. The resulting mixture was stirred at 60 C for 16 hours and then at 70 Cfor additional 7 hours. The solvent was evaporated in vacuo and The residue obtained after the workup was purified by column chromatography (hexane/acetone, 1 : 1) and then by preparative TLC (dichlorome thane/ethyl acetate, 1 :4). The product was obtained as a colorless wax (2 mg, 2 %). (0130) NMR (500 MHz, CDC13) d (ppm) 9.96 (s, 1H), 8.30 (d, / = 5.04 Hz, 1H), 8.27 (s, 1H), 7.34 (d, / = 3.55 Hz, 1H), 7.29 (d, / = 2.11 Hz, 1H), 7.23 (d, / = 8.31 Hz, 1H), 7.10 (dd, / = 8.33, 2.13 Hz, 1H), 6.95 (d, / = 4.99 Hz, 1H), 6.18 (d, / = 3.58 Hz, 1H), 3.94 (tt, / = 11.92, 3.68 Hz, 1H), 2.11 - 2.00 (m, 2H), 1.86 - 1.65 (m, 5H), 1.24 - 1.09 (m, 3H). (0131) 13C NMR (126 MHz, CDC13) d (ppm) 147.5, 141.5, 135.2, 134.9, 134.6, 133.0, 130.9, 130.2, 129.9, 127.2, 127.0, 120.8, 117.4, 100.4, 56.6, 35.3, 34.3, 25.7, 25.7, 25.1.
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